A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674064



Internal ID9593483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:59149388..59149687hg38UCSC Ensembl
Outerchr11:59149351..59149737hg38UCSC Ensembl
Innerchr11:58916861..58917160hg19UCSC Ensembl
Outerchr11:58916824..58917210hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5906888
SamplesNA18550
Known GenesFAM111A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674064
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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